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Summary Literature (0)
MIM:236670 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1

Xenbase Genes: large1, pomt1, fktn, pomt2, fkrp

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000171 - respiration organ
MONDO:0009364 - muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1
MONDO:0018939 - muscle-eye-brain disease

Disease Ontology (DO):
DOID:0050560 - Walker-Warburg syndrome